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Xavier Ferrer

Affiliation : Hôpital Cardiologique du Haut-Lévêque

• 1Publications (affiliation in France)
• 141Total publications
• 5503Citations
• 35h-index

ORCIDOpenAlex

Research profile

Xavier Ferrer has 1 indexed publication (2009). Their work appears in “Journal of Neurology”. Their most cited article, “Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7” (2009), has been cited 81 times. Their work is co-authored with at least 12 researchers.

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Research areas

• Peripheral Neuropathies and Disorders
• Hereditary Neurological Disorders
• Muscle Physiology and Disorders
• Genetic Neurodegenerative Diseases
• Genomics and Rare Diseases

Publications (1)

• Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7
  2009 · Journal of Neurology · cited 81 times

Collaborations

Partner institutions : Institut de Myologie · Pitié-Salpêtrière Hospital · Assistance Publique – Hôpitaux de Paris · Inserm · Université Pierre-et-Marie-Curie

Co-authors

• Francois Michael Petit
• Philippe Petiot
• Michel Fardeau
• David Orlikowski
• L. Lazaro
• Andrée Rouche
• Pascale Richard
• Gisela Stoltenburg
• Daniel Hantaı̈
• Marion Paturneau-Jouas
• B. Eymard
• Fabien Zagnoli

Bibliographic data from OpenAlex (open database).